A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012653



Internal ID19101870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3912156..4117947hg38UCSC Ensembl
Innerchr4:3913883..4119674hg19UCSC Ensembl
Innerchr4:3964803..4170575hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38205792
hg19205792
hg18205773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5089n100
Supporting Variantsnssv3616158
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012653
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer